What would be the best choices for the missing reagents 1 and 3 in this synthesis?1. PPh33122. n-BuLi• Draw the missing reagents in the drawing area below. You can draw them in any arrangement you like.• Do not draw the missing reagent 2. If you draw 1 correctly, we'll know what it is.• Note: if one of your reagents needs to contain a halogen, use bromine.ExplanationCheckClick and drag to start drawing a structure.2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Priva×

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Answered: What would be the best choices for the…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter19: Eas: Electrophilic Aromatic Substitution

Section: Chapter Questions

Problem 3CTQ

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Is the product of this reaction more or less soluble than the initial molecule? Why? 1. RCO;H 2. H*, H,O Less water-soluble More water-soluble Water-solubility improved due to a negative charge on the product. Water-solubility improved due to a positive charge on the product. The product now has sufficient H-bonding functional groups to support water-solubility. An acetal has been formed which would decrease the water-solubility Another reason
Draw an alkyl bromide that would produce ONLY the following alkene in an E2 elimination. Ignore any inorganic byproducts.
The following molecules are subject to substitution (SN1 or SN2) reaction conditions. a) Identify if the leaving group (-Br) is attached to a 3°, 2°, 1°, or methyl Carbon. b) Rank the molecule with respect to their SN1 reactivity, with 1 being the fastest and 4 being the slowest. c) Rank the molecule with respect to their SN2 reactivity, with 1 being the fastest and 4 being the slowest. Br Br CH3B Br a. type of Carbon on C-Br b. SN1 reactivity (1 fastest, 4 slowest) c. SN2 reactivity (1 fastest, 4 slowest)
Please answer both
5. a) When compound 5 is treated with methanol it forms a carbocation. Draw the carbocation that would be formed and the best resonance structure of the compound. CH3 5 CH3OH Br b) Below are different conditions that can be used for an SN1 mechanism. In each pair circle the molecule that would provide a faster SN1. If they are equal rates, circle both. a) electrophile b) solvent c) Nucleophile CH3OH CH3OH CH3ONa
Draw the major organic product(s) of the following reaction. CI + NaOCH3 CH3OH • You do not have to consider stereochemistry. • If no reaction occurs, draw the organic starting material. • When SN1 & E1 pathways compete, show both the substitution and the elimination products. Separate multiple products using the + sign from the drop-down menu. • Do not include counter-ions, e.g., Na+, I, in your answer.
Show how you might synthesize this compound from an alkyl bromide and a nucleophile in an SN2 reaction. / من • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Only draw the reactants. Separate multiple reactants using the + sign from the drop-down menu. • If there is more than one possible combination of alkyl bromide and nucleophile, draw only one combination. • Do not include counter-ions, e.g., Na+, I, in your answer. Submit Answer N3 ? ChemDoodle Retry Entire Group ▼n n [ ]# 8 more group attempts remaining
Complete the following synthesis by filling in the missing reactants, reagents, and products.• Boxes with sharp corners are structures; rounded corners are reagents (may be written or drawn).• Reagent boxes may hold multiple reagents/steps.
1. In each case, provide the product according to the request, Markovnikov or Anti-Markovnikov. We are just practicing the proper placement of the atoms across the double bond. Actual reaction conditions or stereochemistry are not being considered. Add H and Cl Add H and OH Markovnikov Anti-Markovnikov Add H and Br Add H and Br Anti-Markovnikov Anti-Markovnikov Add H and OH Add H and Cl Markovnikov Markovnikov Add H and Br Add H and OH Anti-Markovnikov Markovnikov
Draw the least stable resonance form for the intermediate in the following electrophilic substitution reaction. CF3 CF3 Br2/FeBr3 • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. Br In cases where there is more than one answer, just draw one. Br F ?
If CH3CH20 is to be used as a nucleophile, then what alcohol would be an appropriate solvent? The transform below undoes a nucleophilic substitution reaction. How would you carry out the reaction in the forward direction using a protic solvent? CH3 Undo a CH3 nucleophilic substitution.
please answer the bottom three questions for both reactions

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